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Arteriosclerosis, Thrombosis, and Vascular Biology. 1995;15:1419-1423

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(Arteriosclerosis, Thrombosis, and Vascular Biology. 1995;15:1419-1423.)
© 1995 American Heart Association, Inc.


Articles

Presence and Formation of `Free Apolipoprotein A-I–Like' Particles in Human Plasma

Bela F. Asztalos; Paul S. Roheim

From Louisiana State University Medical Center, Division of Lipoprotein Metabolism and Pathophysiology, Department of Physiology, New Orleans, La.

Correspondence to Paul S. Roheim, MD, Louisiana State University Medical Center, Department of Physiology, 1542 Tulane Ave, New Orleans, LA 70112-2822.

Abstract The influence of dilution on apolipoprotein (apo) A-I–containing subpopulations was studied in human plasma. Agarose electrophoresis and two-dimensional agarose nondenaturing gradient polyacrylamide gel electrophoresis were used. Both in one- and two-dimensional electrophoresis, an increase of charge was observed that resulted in an increase of subpopulations with pre-{alpha} mobility. Dilution of plasma also resulted in a decrease in the size of apo A-I–containing pre-ß1 subpopulations. The existence of smaller pre-ß1 particles was confirmed by subjecting undiluted and 8x diluted plasma to 3% to 16% nondenaturing gradient gel electrophoresis for 4 hours. In addition to the generally observed pre-ß1 subpopulations, smaller particles similar in size to the free apo A-I were detected even in the undiluted plasma. During dilution, the proportion of larger pre-ß1 particles decreased while the smaller ones increased, and in 8x diluted plasma, almost all the pre-ß1 was present in smaller sizes. Using 3% to 35% nondenaturing polyacrylamide gels run for 24 hours, no pre-ß1 particles could be detected in 8x diluted plasma because the small pre-ß1 electrophoresed out. These studies show that pre-ß1 particles can be converted to smaller ones during dilution. It also was demonstrated that "free apo A-I–like" pre-ß1 particles are present in undiluted plasma. The presence of these particles may have important physiological and pathophysiological functions.


Key Words: apolipoproteins • plasma • electrophoresis




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